Regulatory Affairs Specialist

Location: London.

Contract: Full Time.

Industry: Pharmaceutical.

Salary: Competitive.


  • Development of regulatory documentation and timely submissions to regulatory authorities.
  • Manage and conduct communications with external regulatory authorities and ensure positive and trusted relationships are developed.
  • Ensure regulatory plans are established and followed to support future pharmaceutical licensing applications.
  • Work collaboratively to ensure robust studies are planned and carried out to the required regulatory standards.


  • BSc or advanced degree in any relevant scientific field.
  • Prior regulatory affairs experience in pharmaceutical development.
  • Good knowledge of clinical trial regulations.
  • Ability to multitask and prioritize.
  • Prepare and manage clinical trial applications.
  • Interpersonal and communication skills.
  • Proofreading, editing, and technical system skills.

I am looking forward to having a chat with you if you are suitable for this role. For more information on this exciting opportunity please email a copy of your CV in MS WORD format to using Regulatory Affairs Specialist as the Subject.

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Job Category: Doctors
Job Location: London

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